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Fosfomycin tromethamine

Product Name
Fosfomycin tromethamine
CAS No.
78964-85-9
Chemical Name
Fosfomycin tromethamine
Synonyms
FOSFOMYCIN TROMETAMOL;FOSFOMYCIN TROMETHAMOL;phosphomycin trometamol;tromethamine-fosfomycin;z1282;monuril;Fosfomycin tromethanol;fosfomycin tromethamine;Fosfomycin Tromethaminel;fosfomycintrometamolsalt
CBNumber
CB9365184
Molecular Formula
C7H18NO7P
Formula Weight
259.19
MOL File
78964-85-9.mol
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Fosfomycin tromethamine Property

Melting point:
122-125oC
storage temp. 
Hygroscopic, Refrigerator, under inert atmosphere
solubility 
Very soluble in water, slightly soluble in ethanol (96 per cent) and in methanol, practically insoluble in acetone.
form 
Solid
color 
White to Off-White
Stability:
Hygroscopic
InChIKey
QZJIMDIBFFHQDW-LMLSDSMGSA-N
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Safety

HS Code 
2941906000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

H334May cause allergy or asthma symptoms or breathing difficulties if inhaled

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P272Contaminated work clothing should not be allowed out of the workplace.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P285In case of inadequate ventilation wear respiratory protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P341IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P321Specific treatment (see … on this label).

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P333+P313IF SKIN irritation or rash occurs: Get medical advice/attention.

P342+P311IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician.

P362Take off contaminated clothing and wash before reuse.

P363Wash contaminated clothing before reuse.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
F0400000
Product name
Fosfomycin trometamol
Purity
European Pharmacopoeia (EP) Reference Standard
Packaging
f0400000
Price
$153
Updated
2024/03/01
Sigma-Aldrich
Product number
1286322
Product name
Fosfomycin trometamol
Packaging
800mg
Price
$436
Updated
2024/03/01
Sigma-Aldrich
Product number
SML2512
Product name
Fosfomycin Trometamol
Packaging
20MG
Price
$125
Updated
2023/06/20
Cayman Chemical
Product number
23632
Product name
Fosfomycin Trometamol
Purity
≥98%
Packaging
5mg
Price
$37
Updated
2024/03/01
Cayman Chemical
Product number
23632
Product name
Fosfomycin Trometamol
Purity
≥98%
Packaging
10mg
Price
$65
Updated
2024/03/01
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Fosfomycin tromethamine Chemical Properties,Usage,Production

Chemical Properties

White to off-white powder

Uses

Phosphonic acid derivative; antibacterial.

Uses

Fosfomycin Tromethamine is used as an antibiotic compound in the treatment of urinary tract infections.

Definition

ChEBI: Fosfomycin tromethamine is a phosphonoacetic acid.

brand name

Monurol (Zambon).

General Description

Fosfomycin tromethamine (Monurol) is a phosphonic acidepoxide derivative that was initially isolated from fermentationsof Streptomyces spp. Making the tromethamine salt greatly expanded the therapeutic utility of this antibacterial because water solubilityincreased enough to allow oral administration.
Fosfomycin is a broad-spectrum, bactericidal antibacterialthat inhibits the growth of E. coli, S. aureus, andSerratia, Klebsiella, Citrobacter, Enterococcus, andEnterobacter spp. at a concentration less than 64 mg/L.Currently fosfomycin is recommended as single-dose therapyfor uncomplicated urinary tract infections. It possessesin vitro efficacy similar to that of norfloxacin and trimethoprim-sulfamethoxazole.
Fosfomycin covalently inactivates the first enzyme in thebacterial cell wall biosynthesis pathway, UDP-N-acetylglucosamineenolpyruvyl transferase (MurA) by alkylation ofthe cysteine-115 residue. The inactivation reaction occursthrough nucleophilic opening of the epoxide ring. Resistanceto fosfomycin can occur through chromosomal mutationsthat result in reduced uptake or reduced MurA affinity for theinhibitor. Plasmid-mediated resistance mechanisms involveconjugative bioinactivation of the antibiotic with glutathione.The frequency of resistant mutants in in vitro studies hasbeen low, and there appears to be little cross-resistance betweenfosfomycin and other antibacterials.

Fosfomycin tromethamine Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Fosfomycin tromethamine manufacturers

airuikechemical co., ltd.
Product
Fosfomycin Tromethamine 78964-85-9
Price
US $0.00-0.00/Kg
Min. Order
1Kg
Purity
99.9%
Supply Ability
200tons
Release date
2024-04-08
Hebei Duling International Trade Co. LTD
Product
Fosfomycin tromethamine 78964-85-9
Price
US $100.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
100 tons
Release date
2023-01-11
Hebei Yanxi Chemical Co., Ltd.
Product
Fosfomycin Tromethamine 78964-85-9
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
3000kg
Release date
2023-08-11

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